HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 22414444, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-amino-N-formyl-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamine | HCID 10423492 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22414444 | HCID 22414444 | — |
Reaction Steps
A solution of 5.0 g of 2-amino-N-formyl-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine in 48 ml of acetonitrile was treated with 6.5 ml of a 37% formaldehyde solution and 1.9 g of sodium cyanoborohydride. The mixture was stirred for 1.5 hr and then concentrated. The residue was dissolved in 75 ml of ether and washed with 1N potassium hydroxide solution and with saturated brine. The ether solution was dried over anhydrous potassium carbonate and concentrated. The residue was purified by Preparative HPLC (Waters Associates Prep LC/System 500, silica gel, eluted with ethyl acetate, 200 ml/min, Glo-Mac Model 80-800 UV detector). The appropriate fractions were collected and concentrated to give 3.8 g of product, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292760 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-294537446c1e4d988af467a7ba545d11 |
| Source note | uspto-grants-1994_03 |